Canonical Allele Identifier: PA2828090511
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50010
ClinVar RCV Id: RCV000043278 RCV000421501 RCV000457171 RCV001018037 RCV002262605
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Met286Thr
CA023058
NM_001363528.2:c.857T>C